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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880681Generated: November 1, 2026

1-Pyrrolidinecarbonyl chloride → HCID 59570315, compound

https://huagongshe.com/reaction/1880681

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Pyrrolidinecarbonyl chlorideHCID 70937—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 178517507HCID 178517507—
SolventPyridineHCID 1049—
ProductHCID 59570315HCID 5957031563.4%

Reaction Steps

To 1 ml of pyridine were added 0.3 g of 1,8-diazabicyclo[5,4,0]undec-7-ene, and 0.3 g of 3-(4-trifluoromethylpyridin-2-yl)-1,2,4-oxadiazol-5-one, and 0.26 g of 1-pyrrolidinecarbonyl chloride was added at room temperature. After stirring for 15 hours, the resultant solution was concentrated, and the residue was subjected to silica gel column chromatography to obtain 0.27 g of 4-(1-pyrrolidinecarbonyl)-3-(4-trifluoromethylpyridin-2-yl)-1,2,4-oxadiazol-5-one (present compound (15)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318776B2
Source datasetuspto-grants-2012_11
ORD IDord-4240a185bf3f4d7ab13647fdc03f4353
Source noteuspto-grants-2012_11